3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

Base Information

Chemical Name:3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one
CAS No.:1231749-71-5
Molecular Formula:C₂₆H₃₁N₇O₃
Molecular Weight:489.577
Hs Code.:

Synonyms:3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

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Chemical Property of 3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

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Technology Process of 3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

There total 6 articles about 3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1231749-73-7
3-{1-[6-(4-amino-3-methyl-5-nitro-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

: 1231749-71-5
3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; for 8h; under 2585.81 Torr;

Reference yield:

: 2835-99-6
4-amino-3-methylphenol

: 1231749-71-5
3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: sodium acetate; acetic acid / 1 h / 125 °C

2: nitric acid / 1 h / 10 - 18 °C

3: hydrogenchloride; water / 2 h

4: potassium carbonate / N,N-dimethyl-formamide / 6 h / 50 °C

5: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

6: hydrogen / palladium 10% on activated carbon / methanol / 8 h / 2585.81 Torr

With hydrogenchloride; water; hydrogen; nitric acid; sodium acetate; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In methanol; N,N-dimethyl-formamide;

Reference yield:

: 1231749-72-6
4-(6-chloro-pyrimidin-4-yloxy)-2-methyl-6-nitro-phenylamine

: 1231749-71-5
3-{1-[6-(3,4-diamino-5-methyl-phenoxy)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 8 h / 2585.81 Torr

With hydrogen; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In methanol; N,N-dimethyl-formamide;